Human gingival mesenchymal stem cells retain their growth and immunomodulatory characteristics independent of donor age.
Jay R DaveSayali S ChandekarShubhanath BeheraKaushik U DesaiPradnya M SalveNeha B SapkalSuhas T MhaskeAnkush M DewleParag S PokareMegha PageAjay JogPankaj A ChivteRupesh K SrivastavaGeetanjali B TomarPublished in: Science advances (2022)
Aging has been reported to deteriorate the quantity and quality of mesenchymal stem cells (MSCs), which affect their therapeutic use in regenerative medicine. A dearth of age-related stem cell research further restricts their clinical applications. The present study explores the possibility of using MSCs derived from human gingival tissues (GMSCs) for studying their ex vivo growth characteristics and differentiation potential with respect to donor age. GMSCs displayed decreased in vitro adipogenesis and in vitro and in vivo osteogenesis with age, but in vitro neurogenesis remained unaffected. An increased expression of p53 and SIRT1 with donor age was correlated to their ability of eliminating tumorigenic events through apoptosis or autophagy, respectively. Irrespective of donor age, GMSCs displayed effective immunoregulation and regenerative potential in a mouse model of LPS-induced acute lung injury. Thus, we suggest the potential of GMSCs for designing cell-based immunomodulatory therapeutic approaches and their further extrapolation for acute inflammatory conditions such as acute respiratory distress syndrome and COVID-19.
Keyphrases
- mesenchymal stem cells
- lps induced
- stem cells
- acute respiratory distress syndrome
- umbilical cord
- oxidative stress
- cell therapy
- endothelial cells
- mouse model
- inflammatory response
- cell death
- coronavirus disease
- endoplasmic reticulum stress
- extracorporeal membrane oxygenation
- type diabetes
- gene expression
- induced pluripotent stem cells
- poor prognosis
- mechanical ventilation
- human health
- intensive care unit
- metabolic syndrome
- signaling pathway
- risk assessment
- blood brain barrier
- single cell
- brain injury
- ischemia reperfusion injury
- hepatitis b virus
- respiratory failure
- climate change
- cell proliferation
- pluripotent stem cells